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Strain Name: |
HPT/LeJ |
Stock Number: |
001057 |
Availability:
| Repository-Cryopreserved |
Product Information
Strain Details
| Type |
Inbred Strain |
| Additional information on
Inbred Strains. |
| Type |
JAX® GEMM® Strain -
Spontaneous Mutation |
| Additional information on
JAX® GEMM® Strains. |
| Species | laboratory mouse |
| Generation | F29
|
|
|
Important Note
This strain is homozygous for nonagouti and segregating for Hpt.
Mammalian Phenotype Terms assigned by genotype
Hpt/Hpt
HPT/Le
- lethality-prenatal/perinatal
- prenatal lethality
(MGI Ref ID J:1780)
- die by 6 to 8 days of gestation
- embryonic lethality before somite formation
(MGI Ref ID J:1780)
- death is associated with abnormalities of ectodermal derivatives
Hpt/Hpt+
HPT/Le
- skin/coat/nails phenotype
- abnormal hair follicle development
(MGI Ref ID J:1780)
- follicles may not produce hairs or hairs may not erupt
- keratin plugs follicles
- abnormal follicles are larger than normal
- abnormal hair growth
(MGI Ref ID J:1780)
- patchy absence of hair throughout life
- pigmented and unpigmented areas observed soon after birth correspond to future areas of abnormal and normal hair growth respectively
- abnormal skin pigmentation
(MGI Ref ID J:1780)
- mosaicism for pigmented and unpigmented areas is observed a few days after birth
- decreased hair follicle number
(MGI Ref ID J:1780)
- reduced numbers of normal follicles can be detected as early as E14
- renal/urinary system phenotype
- abnormal kidney morphology
(MGI Ref ID J:1780)
- model for mechanisms of progressive noninflammatory renal disease
- abnormal renal glomerulus morphology
(MGI Ref ID J:1780)
- abnormal podocyte foot process morphology
(MGI Ref ID J:1780)
- disorganization, swelling, and fusion of the foot processes
- fused podocyte foot processes
(MGI Ref ID J:1780)
- glomerulosclerosis
(MGI Ref ID J:1780)
- condition is progressive and by 6 months of age most glomeruli show advanced sclerosis
- kidney failure
(MGI Ref ID J:1780)
- results from progressive glomerulosclerosis
- cardiovascular system phenotype
- enlarged heart
(MGI Ref ID J:1780)
- left ventricle hypertrophy
(MGI Ref ID J:1780)
- hypertension
(MGI Ref ID J:1780)
- increased systolic pressure by 3 months of age
- pigmentation phenotype
- abnormal skin pigmentation
(MGI Ref ID J:1780)
- mosaicism for pigmented and unpigmented areas is observed a few days after birth
- hematopoietic system phenotype
- abnormal erythropoiesis
(MGI Ref ID J:1780)
- anemia
(MGI Ref ID J:1780)
- occurs by 40 weeks of age
- assumed secondary to renal failure
- decreased leukocyte cell number
(MGI Ref ID J:1780)
- before one year of age counts are normal
- at 68 weeks of age the leukocyte count is significanlty decreased with a slight decrease in lymphocytes and increase in neutrophils
- growth/size phenotype
- decreased body size
(MGI Ref ID J:1780)
- mutants at all ages are smaller than age and sex-matched controls
- immune system phenotype
- decreased leukocyte cell number
(MGI Ref ID J:1780)
- before one year of age counts are normal
- at 68 weeks of age the leukocyte count is significanlty decreased with a slight decrease in lymphocytes and increase in neutrophils
The following phenotype information may relate to a genetic background differing from this JAX® Mice strain.
Hpt/Hpt
(C57BL/6J x C3FeLe.B6-a/a)F1
- skin/coat/nails phenotype
- abnormal coat appearance
(MGI Ref ID J:13897)
- coat appearance of a homozygote can be discerned from a heterozygote only by breeding tests
- patchy hair
(MGI Ref ID J:13897)
- the permanent coat may be normal with a few bare patches
- sparse hair
(MGI Ref ID J:13897)
- some homozygotes have a sparse permanent coat with extensive bare patches
- abnormal hair follicle development
(MGI Ref ID J:13897)
- abnormal skin pigmentation
(MGI Ref ID J:13897)
- pigmentation phenotype
- abnormal skin pigmentation
(MGI Ref ID J:13897)
Hpt/Hpt+
(C57BL/6J x C3FeLe.B6-a/a)F1
- skin/coat/nails phenotype
- abnormal coat appearance
(MGI Ref ID J:13897)
- patchy hair
(MGI Ref ID J:13897)
- permanent coat of some may be normal but have a few bare patches
- sparse hair
(MGI Ref ID J:13897)
- the permanent coat of some heterozygotes is sparse with extensive bare patches
- abnormal hair follicle development
(MGI Ref ID J:13897)
- abnormal skin pigmentation
(MGI Ref ID J:13897)
- the skin is littered with heavily pigmented debris
- pigmentation phenotype
- abnormal skin pigmentation
(MGI Ref ID J:13897)
- the skin is littered with heavily pigmented debris
|
Gene & Allele Details
| Allele Symbol |
Hpt |
| Allele Name |
hair patches |
| Common Name(s) |
Hpa;
|
| Strain of Origin | (C57BL/6J x C3FeLe.B6-a/a)F1 |
| |
| Allele Symbol |
a |
| Allele Name |
nonagouti |
Control Information
Related Strains
Strains carrying a allele
View Strains carrying a (102 strains)
Strains carrying other alleles of a
View Strains carrying other alleles of a (67 strains)
Research Applications
This mouse can be used to support research in many areas including:
Hpt related
Dermatology Research
Color and White Spotting Defects
References
Additional References
Price and Supply Information
| Strain Name: |
HPT/LeJ |
| Stock Number: |
001057 |
Price Details
IMPORTANT NOTE: Prices are based on shipping destination.
The shipping destinations are:
*Pricing for Shipping Destination selected:
International
| Price(s) in US dollars ($) | |
| Cryorecovery Fee | $2470.00 | | | |
Supply Details
| Standard Supply | Repository-Cryopreserved. Must Be Recovered. Please refer to pricing and supply notes for further information. |
| Supply Notes |
Cryorecovery - Standard. The recovery process begins when a signed agreement form is returned to the Customer Service Department after order placement. Although results vary by strain, at least two males and two females (two pairs) will be provided, typically within 15 weeks of our receipt of the signed agreement form. If the first recovery attempt is unsuccessful or only one pair is recovered, a second recovery will be done, extending the delivery time to approximately 25 weeks. At least one member of each pair will be of known genotype and will carry the mutation if it is a mutant strain. Please note that pairs may not reflect the mating scheme utilized by The Jackson Laboratory prior to cryopreservation of the strain. Mating schemes are sometimes modified for successful cryopreservation. Price represents a repository maintenance fee, which includes the cost of recovery of the strain from the cryopreservation resource and the periodic replacement of the frozen embryos used for recovery.
Cryorecovery to establish a Dedicated Supply for greater quantities of mice. One to two pairs will be recovered to establish a Dedicated Supply of mice. Price by quotation. For more information on Dedicated Supply, please contact JAX® Services: Tel: 1-800-422-6423 or 1-207-288-5845; Email: jaxservices@jax.org.
Genomic DNA is available for this strain from the Mouse DNA Resource.
|
| Licensing | See General Terms and Conditions below
|
| Control Information | View Control Information in Strain Details.
View Control Pricing Information for JAX® Strains. |
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JAX® Mice & Services Conditions of Use.
The Jackson Laboratory's Genotype Promise
The Jackson Laboratory has rigorous genetic quality control and mutant gene
genotyping programs to ensure the genetic background of JAX
® Mice strains as
well as the genotypes of strains with identified molecular mutations.
JAX
® Mice strains are only made available to researchers after meeting our
standards. However, the phenotype of each strain may not be fully
characterized and/or captured in the strain data sheets.
Therefore, we
cannot guarantee a strain's phenotype will meet all expectations. To
ensure that JAX
® Mice will meet the needs of individual research projects
or when requesting a strain that is new to your research, we suggest ordering
and performing tests on a small number of mice to determine suitability for
your particular project.
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